UTP14C
Description
The UTP14C (UTP14C small subunit processome component) is a protein-coding gene located on chromosome 13.
UTP14C is also known as 2700066J21Rik, KIAA0266, UTP14B.
Associated Diseases
- congenital disorder of glycosylation
- ALG11-congenital disorder of glycosylation
- partial chromosome Y deletion
- male infertility with teratozoospermia due to single gene mutation
- spermatogenic failures 50
- spermatogenic failure 25
- spermatogenic failure, X-linked, 2
- spermatogenic failure 61
- spermatogenic failure 73
- spermatogenic failure 74
- spermatogenic failure 48
- congenital bilateral absence of vas deferens
- spinocerebellar ataxia type 32
- spermatogenic failure 23
- spermatogenic failure 52
- deafness-infertility syndrome
- spermatogenic failure 22
